Literature DB >> 27155484

Metabolic effects of azoxystrobin and kresoxim-methyl against Fusarium kyushuense examined using the Biolog FF MicroPlate.

Hancheng Wang1, Jin Wang2, Qingyuan Chen1, Maosheng Wang1, Tom Hsiang3, Shenghua Shang1, Zhihe Yu4.   

Abstract

Azoxystrobin and kresoxim-methyl are strobilurin fungicides, and are effective in controlling many plant diseases, including Fusarium wilt. The mode of action of this kind of chemical is inhibition of respiration. This research investigated the sensitivities of Fusarium kyushuense to azoxystrobin and kresoxim-methyl, and to the alternative oxidase inhibitor salicylhydroxamic acid (SHAM). The Biolog FF MicroPlate is designed to examine substrate utilization and metabolic profiling of micro-organisms, and was used here to study the activity of azoxystrobin, kresoxim-methyl and SHAM against F. kyushuense. Results presented that azoxystrobin and kresoxim-methyl strongly inhibited conidial germination and mycelial growth of F. kyushuense, with EC50 values of 1.60 and 1.79μgml(-1), and 6.25 and 11.43μgml(-1), respectively; while not for SHAM. In the absence of fungicide, F. kyushuense was able to metabolize 91.6% of the tested carbon substrates, including 69 effectively and 18 moderately. SHAM did not inhibit carbon substrate utilization. Under the selective pressure of azoxystrobin and kresoxim-methyl during mycelial growth (up to 100μgml(-1)) and conidial germination (up to 10μgml(-1)), F. kyushuense was unable to metabolize many substrates in the Biolog FF MicroPlate; while especially for carbon substrates in glycolysis and tricarboxylic acid cycle, with notable exceptions such as β-hydroxybutyric acid, y-hydroxybutyric acid, α-ketoglutaric acid, α-d-glucose-1-phosphate, d-saccharic acid and succinic acid in the mycelial growth stage, and β-hydroxybutyric acid, y-hydroxybutyric acid, α-ketoglutaric acid, tween-80, arbutin, dextrin, glycerol and glycogen in the conidial germination stage. This is a new finding for some effect of azoxystrobin and kresoxim-methyl on carbon substrate utilization related to glycolysis and tricarboxylic acid cycle and other carbons, and may lead to future applications of Biolog FF MicroPlate for metabolic effects of other fungicides and other fungi, as well as providing a carbon metabolic fingerprint of F. kyushuense that could be useful for identification.
Copyright © 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Azoxystrobin; Biolog FF MicroPlate; Kresoxim-methyl; Mode of action; Sensitivity

Mesh:

Substances:

Year:  2015        PMID: 27155484     DOI: 10.1016/j.pestbp.2015.11.013

Source DB:  PubMed          Journal:  Pestic Biochem Physiol        ISSN: 0048-3575            Impact factor:   3.963


  3 in total

1.  Metabolic activities of five botryticides against Botrytis cinerea examined using the Biolog FF MicroPlate.

Authors:  Hancheng Wang; Jin Wang; Licui Li; Tom Hsiang; Maosheng Wang; Shenghua Shang; Zhihe Yu
Journal:  Sci Rep       Date:  2016-08-05       Impact factor: 4.379

2.  Metabolic Phenotype Characterization of Botrytis cinerea, the Causal Agent of Gray Mold.

Authors:  Han-Cheng Wang; Li-Cui Li; Bin Cai; Liu-Ti Cai; Xing-Jiang Chen; Zhi-He Yu; Chuan-Qing Zhang
Journal:  Front Microbiol       Date:  2018-03-13       Impact factor: 5.640

Review 3.  Natural Products from Medicinal Plants against Phytopathogenic Fusarium Species: Current Research Endeavours, Challenges and Prospects.

Authors:  Hlabana A Seepe; Winston Nxumalo; Stephen O Amoo
Journal:  Molecules       Date:  2021-10-29       Impact factor: 4.411

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.